The co-occurrence of epilepsy and autism: A systematic review
Sara Lukmanji1, Sofiya A Manji1, Sandra Kadhim1
1Department of Clinical Neurosciences, Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, Canada.
Insights
Autism and epilepsy frequently co-occur. This review found higher prevalence rates of epilepsy in autism (12.1%) and autism in epilepsy (9.0%) than previously estimated, highlighting the need for screening.
Area of Science:
- Neurology
- Developmental Neuroscience
- Epidemiology
Background:
- Autism Spectrum Disorder (ASD) and epilepsy are frequently comorbid neurological conditions.
- Understanding the prevalence of these co-occurring conditions is crucial for clinical management and research.
Purpose of the Study:
- To systematically review and synthesize the existing literature on the incidence and prevalence of autism in epilepsy and epilepsy in autism.
- To provide updated estimates for these comorbid conditions.
Main Methods:
- A systematic literature search was conducted across multiple databases (MEDLINE, Embase, PsycINFO, Cochrane) adhering to PRISMA standards.
- Studies reporting prevalence or incidence of autism in epilepsy or epilepsy in autism were included.
- Data were analyzed using descriptive statistics, including median and interquartile range, with meta-regression to assess study quality impact.
Main Results:
- Seventy-four studies encompassing 283,549 patients were included.
- The median overall period prevalence was 12.1% for epilepsy in autism and 9.0% for autism in epilepsy.
- Excluding syndromic epilepsy or developmental delay cases yielded prevalences of 11.2% and 8.1%, respectively. Sex-based prevalence trends were observed.
Conclusions:
- The prevalence of epilepsy in individuals with autism, and autism in individuals with epilepsy, is higher than previously reported general population estimates.
- These findings underscore the importance of screening for epilepsy in individuals with autism and for autism in individuals with epilepsy.
- The results may offer insights into the shared underlying mechanisms (pathogenesis) of these two conditions.
Objective:
We aimed to review the literature to determine the incidence and prevalence of autism in epilepsy and epilepsy in autism, conditions that are often comorbid.
Methods:
We adhered to the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) standards, and the protocol was registered with PROSPERO. MEDLINE, Embase, PsycINFO, and the Cochrane Database of Systematic Reviews were searched from inception until July 4, 2016. Studies were included if they reported an incidence or prevalence of autism in epilepsy or epilepsy in autism. These estimates were described using mean, standard deviation, median, and interquartile range.
Results:
Seventy-four studies reporting on 283,549 patients were included. The median overall period prevalence of epilepsy in people with autism was 12.1% while the median overall period prevalence of autism in people with epilepsy was 9.0% when including all population types. When excluding studies that investigated patients with syndromic epilepsy or developmental delay, the median overall period prevalence of epilepsy in people with autism was 11.2% while the median overall period prevalence of autism in people with epilepsy was 8.1%. We observed trends for sex as the prevalence of autism in epilepsy was higher in males while the prevalence of epilepsy in autism was higher in females. It is important to interpret these estimates with caution, as there was significant heterogeneity between studies. Meta-regression found no association between study quality and prevalence or incidence estimates (all p-values > 0.05).
Conclusions:
The period prevalence of epilepsy in people with autism, and vice versa, was consistently higher than previously reported estimates of the occurrence of these disorders in the general population. These findings highlight the importance of screening for autism in people who have epilepsy and epilepsy in people who have autism and may help shed light on shared pathogenesis between these conditions.
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